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Pan-Cancer Analysis Identified C1ORF112 as a Potential Biomarker for Multiple Tumor Types

C1ORF112 is an evolutionarily conserved gene across vertebrates. Over the last decade, studies have suggested that C1ORF112 may play a role in tumorigenesis. Using The Cancer Genome Atlas datasets, we explored the role of C1ORF112 across various tumor types in this study. In most tumor types, C1ORF1...

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Autores principales: Chen, Jiaxuan, Mai, Haoming, Chen, Haitao, Zhou, Bin, Hou, Jinlin, Jiang, De-Ke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8416665/
https://www.ncbi.nlm.nih.gov/pubmed/34490347
http://dx.doi.org/10.3389/fmolb.2021.693651
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author Chen, Jiaxuan
Mai, Haoming
Chen, Haitao
Zhou, Bin
Hou, Jinlin
Jiang, De-Ke
author_facet Chen, Jiaxuan
Mai, Haoming
Chen, Haitao
Zhou, Bin
Hou, Jinlin
Jiang, De-Ke
author_sort Chen, Jiaxuan
collection PubMed
description C1ORF112 is an evolutionarily conserved gene across vertebrates. Over the last decade, studies have suggested that C1ORF112 may play a role in tumorigenesis. Using The Cancer Genome Atlas datasets, we explored the role of C1ORF112 across various tumor types in this study. In most tumor types, C1ORF112 expression was increased in tumor tissues compared to corresponding non-tumor tissues. In patients with certain tumor types, higher C1ORF112 expression was correlated with shorter overall survival, disease-free survival, and progression-free survival. Further analyses of C1ORF112 genetic alteration data showed that C1ORF112 amplification and mutations may have an impact on liver hepatocellular carcinoma and uterine corpus endometrial carcinoma prognosis. In cancers including lower grade glioma and adrenocortical carcinoma, C1ORF112 expression was linked to cancer-associated fibroblast infiltration. Gene Ontology analysis showed that C1ORF112 was co-expressed with genes involved in biological processes such as cell cycle and mitotic regulation. The protein interaction network demonstrated that C1ORF112 physically interacted with RAD51, DMC1, and FIGNL1, which have well characterized functions in DNA repair and cell cycle regulation. This pan-cancer study revealed the prognostic value and oncogenic role of C1ORF112 across multiple tumor types.
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spelling pubmed-84166652021-09-05 Pan-Cancer Analysis Identified C1ORF112 as a Potential Biomarker for Multiple Tumor Types Chen, Jiaxuan Mai, Haoming Chen, Haitao Zhou, Bin Hou, Jinlin Jiang, De-Ke Front Mol Biosci Molecular Biosciences C1ORF112 is an evolutionarily conserved gene across vertebrates. Over the last decade, studies have suggested that C1ORF112 may play a role in tumorigenesis. Using The Cancer Genome Atlas datasets, we explored the role of C1ORF112 across various tumor types in this study. In most tumor types, C1ORF112 expression was increased in tumor tissues compared to corresponding non-tumor tissues. In patients with certain tumor types, higher C1ORF112 expression was correlated with shorter overall survival, disease-free survival, and progression-free survival. Further analyses of C1ORF112 genetic alteration data showed that C1ORF112 amplification and mutations may have an impact on liver hepatocellular carcinoma and uterine corpus endometrial carcinoma prognosis. In cancers including lower grade glioma and adrenocortical carcinoma, C1ORF112 expression was linked to cancer-associated fibroblast infiltration. Gene Ontology analysis showed that C1ORF112 was co-expressed with genes involved in biological processes such as cell cycle and mitotic regulation. The protein interaction network demonstrated that C1ORF112 physically interacted with RAD51, DMC1, and FIGNL1, which have well characterized functions in DNA repair and cell cycle regulation. This pan-cancer study revealed the prognostic value and oncogenic role of C1ORF112 across multiple tumor types. Frontiers Media S.A. 2021-08-19 /pmc/articles/PMC8416665/ /pubmed/34490347 http://dx.doi.org/10.3389/fmolb.2021.693651 Text en Copyright © 2021 Chen, Mai, Chen, Zhou, Hou and Jiang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Molecular Biosciences
Chen, Jiaxuan
Mai, Haoming
Chen, Haitao
Zhou, Bin
Hou, Jinlin
Jiang, De-Ke
Pan-Cancer Analysis Identified C1ORF112 as a Potential Biomarker for Multiple Tumor Types
title Pan-Cancer Analysis Identified C1ORF112 as a Potential Biomarker for Multiple Tumor Types
title_full Pan-Cancer Analysis Identified C1ORF112 as a Potential Biomarker for Multiple Tumor Types
title_fullStr Pan-Cancer Analysis Identified C1ORF112 as a Potential Biomarker for Multiple Tumor Types
title_full_unstemmed Pan-Cancer Analysis Identified C1ORF112 as a Potential Biomarker for Multiple Tumor Types
title_short Pan-Cancer Analysis Identified C1ORF112 as a Potential Biomarker for Multiple Tumor Types
title_sort pan-cancer analysis identified c1orf112 as a potential biomarker for multiple tumor types
topic Molecular Biosciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8416665/
https://www.ncbi.nlm.nih.gov/pubmed/34490347
http://dx.doi.org/10.3389/fmolb.2021.693651
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